Writing for the Medical Device Regulated Industry

Writing for the Medical Device Regulated Industry
ONLINE REGISTRATION FOR THIS WEBINAR IS NOW CLOSED. Are you a new writer for medical devices, or interested in learning more about this exciting industry? All medical devices, regardless of classification, require instructions for use, or labeling. Labeling is typically created by a combination of technical writers, regulatory specialists, engineers and manufacturing personnel. This is becoming a niche area for technical writers, especially those who know and understand the regulations that govern the labeling requirements. Join us for this webinar to learn the basics of developing labeling for medical devices.
2/28/2018 - 2/28/2018

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